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4-methoxyphenyl (2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside | 1237748-34-3

中文名称
——
中文别名
——
英文名称
4-methoxyphenyl (2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
英文别名
Bn(-2)[Bn(-3)][Bn(-6)]Gal(a1-3)[Bn(-2)][Bn(-4)][Bn(-6)]Gal(b)-O-Ph(4-OMe);(2R,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6R)-2-(4-methoxyphenoxy)-3,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-4-yl]oxy-4,5-bis(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-ol
4-methoxyphenyl (2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside化学式
CAS
1237748-34-3
化学式
C61H64O12
mdl
——
分子量
989.172
InChiKey
PEJCRAJDFONRRX-RMDKUHKQSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    9.2
  • 重原子数:
    73
  • 可旋转键数:
    25
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    122
  • 氢给体数:
    1
  • 氢受体数:
    12

反应信息

  • 作为反应物:
    描述:
    4-methoxyphenyl (2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 、 ethyl 2,3-di-O-acetyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 在 N-碘代丁二酰亚胺三氟甲磺酸 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以81%的产率得到4-methoxyphenyl (2,3-di-O-acetyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
    参考文献:
    名称:
    Concise synthesis of a hexasaccharide present in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b
    摘要:
    Concise chemical synthesis of a hexasaccharide repeating unit found in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b was achieved in excellent yield. A [3+3] block synthetic strategy has been applied for the construction of the target hexasaccharide. During the synthesis, the orthogonal property of thioglycosides has been successfully exploited. Yields were high in all intermediate steps. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2010.03.042
  • 作为产物:
    描述:
    4-methoxyphenyl (2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 在 三乙基硅烷 作用下, 以 二氯甲烷 为溶剂, 反应 0.25h, 以75%的产率得到4-methoxyphenyl (2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside
    参考文献:
    名称:
    Concise synthesis of a hexasaccharide present in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b
    摘要:
    Concise chemical synthesis of a hexasaccharide repeating unit found in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b was achieved in excellent yield. A [3+3] block synthetic strategy has been applied for the construction of the target hexasaccharide. During the synthesis, the orthogonal property of thioglycosides has been successfully exploited. Yields were high in all intermediate steps. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2010.03.042
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文献信息

  • Concise synthesis of a hexasaccharide present in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b
    作者:Samir Ghosh、Anup Kumar Misra
    DOI:10.1016/j.tetasy.2010.03.042
    日期:2010.4
    Concise chemical synthesis of a hexasaccharide repeating unit found in the cell wall lipopolysaccharide of Azospirillum lipoferum Sp59b was achieved in excellent yield. A [3+3] block synthetic strategy has been applied for the construction of the target hexasaccharide. During the synthesis, the orthogonal property of thioglycosides has been successfully exploited. Yields were high in all intermediate steps. (C) 2010 Elsevier Ltd. All rights reserved.
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